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Showing articles 0 to 14 of 14 Filter Applied: mitochondrial disease (Click to remove) Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023 Pyruvate Dehydrogenase Deficiency (PDCD) eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018 A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017 Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016 Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease) Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014 Heterogeneity of Coenzyme Q10 Deficiency Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012 A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia Neurol 72:1262-1276, DiMauro,S.,et al, 2009 Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 Acute Leukoencephalopathies:Differential Diagnosis and Investigation The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998 Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996 Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Inclusion Body Myositis and Myopathies Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995 Progressive Dystonia with Bilateral Putaminal Hypodensities Arch Neurol 44:1184-1187, Berkovic,S.F.,et al, 1987 Showing articles 0 to 14 of 14